Building a zoo of mice for genetic analyses: A comprehensive protocol for the rapid generation of BAC transgenic mice
Transgenic mice are highly valuable tools for biological research as they allow cell type–specific expression of functionally instrumental genes. In this protocol, the generation of bacterial artificial chromosome (BAC) transgenic constructs is described. We give an overview of different transgenic...
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Published in: | Genesis (New York, N.Y. : 2000) Vol. 48; no. 4; pp. 264 - 280 |
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Main Authors: | , , , , , , |
Format: | Journal Article |
Language: | English |
Published: |
Hoboken
Wiley Subscription Services, Inc., A Wiley Company
01-04-2010
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Subjects: | |
Online Access: | Get full text |
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Summary: | Transgenic mice are highly valuable tools for biological research as they allow cell type–specific expression of functionally instrumental genes. In this protocol, the generation of bacterial artificial chromosome (BAC) transgenic constructs is described. We give an overview of different transgenic inserts, such as fluorescent proteins (alone or in combination with Cre variants), diphtheria toxin receptor, lacZ, and light‐activated ion channels. The most reliable and versatile approach to express these genes is by using BACs, which allow “highjacking” of the expression pattern of a gene without characterizing its transcriptional control elements. Here, we describe the necessary cloning techniques compared with conventional transgenesis. With the provided “toolbox” of already available transgene constructs, the generation of the BAC transgenes is made easy and rapid. We provide a comprehensive outline how to insert the different transgenes into a chosen BAC by either ET cloning or recombineering. We also describe in detail the methods to identify the correct insertion and the integrity of the final BAC construct, and finally, the preparation of the BAC DNA for oocyte injection is described. genesis 48:264–280, 2010. © 2010 Wiley‐Liss, Inc. |
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Bibliography: | ArticleID:DVG20612 NCCR-Neuro (CTE) istex:9D94FA6724DFCCD2EF0849D632B0F59493C90576 Deutsche Forschungsgemeinschaft - No. BU 1410/1-2 ark:/67375/WNG-1CXQHWKZ-M Swiss National Science Foundation - No. 310000-116201/1; No. CRSI33_125073; No. 3100A0-116064/1; No. 3100A0-116070/1 Torbjörn Johansson and Ilja Broll contributed equally to this work. ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 23 ObjectType-Article-1 ObjectType-Feature-2 |
ISSN: | 1526-954X 1526-968X |
DOI: | 10.1002/dvg.20612 |